E3330 - ≥97% , DNA-(apurinic or apyrimidinic site) lyase inhibitor, CAS No.136164-66-4, DNA-(apurinic or apyrimidinic site) lyase inhibitor

CAS: 136164-66-4 Cat. No.: E413754 Formule: C21H30O6 Poids moléculaire: 378.46 Numéro CE: 693-030-4
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ ≥97%
Synonyms
E3330 | E-3330 | EX-A2212 | Undecanoic acid, 2-((4,5-dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene)-, (E)- | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene]undecanoic acid | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-d
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
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Taille
Allemagne (EU)
USA*
Prix
Qté
5mg
E413754-5mg
—
4 En stock
110,98€
25mg
E413754-25mg
—
2 En stock
332,26€
50mg
E413754-50mg
—
1 En stock
604,73€
100mg
E413754-100mg
—
1 En stock
1 057,69€
250mg
E413754-250mg
—
1 En stock
1 735,39€
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Pourquoi cette qualité

≥97% pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at -20°C Expédition Ice chest + Ice pads. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 0 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Product Describtion:

E3330 (APX-3330) is a direct, orally active and selective inhibitor of Ape-1 (apurinic/apyrimidinic endonuclease 1)/Ref-1 (redox factor-1) redox. E3330 is able to impair tumor growth and blocks the activity of NF-κB, AP-1, and HIF-1α in pancreatic cancer. E3330 shows anticancer activities.


Information

E3330 E3330 (APX-3330) is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.


Targets

NF-κB ; APE1(Ref-1)


In vitro

E3330 affects hemangioblast development in vitro via inhibition of Ape1 redox activity. E3330 inhibits the growth of human pancreatic cancer cell line PANC1, XPA1, MIAPACA, BxPC3, and PK9. E3330 also promotes exit of cell cycle in PANC1 cells, inhibits the DNA-Binding activity of HIF-1α and migration of pancreatic cancer cells. In JHH6 cells, E3330 prevents the functional activation of NF-κB via the alteration of APE1 subcellular trafficking and reduces IL-6 and IL-8 expression induced by TNF-α and FAs accumulation through blockage of the redox-mediated activation of NF-κB.


In vivo

In mice with endotoxin-mediated hepatitis, E3330 (300 mg/kg, p.o.) attenuates the elevation of plasma tumor necrosis factor activity and protectes mice from liver injury. In Rat model, E3330 (100 mg/kg, p.o.) also protectes rats from severe liver injury induced with endotoxin plus galactosamine.


Cell Research(from reference)

Cell lines:PANC1 cells 

Concentrations:~30 μM 

Incubation Time:72 hours 

Spécifications

Synonymes
E3330 | E-3330 | EX-A2212 | Undecanoic acid, 2-((4,5-dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene)-, (E)- | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-dioxo-1,4-cyclohexadien-1-yl)methylene]undecanoic acid | (2E)-2-[(4,5-Dimethoxy-2-methyl-3,6-d
Spécifications et pureté
≥97%
Mécanismes biochimiques et physiologiques
E3330 (APX-3330) is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Type d'action
INHIBITOR
Mécanisme d'action
DNA-(apurinic or apyrimidinic site) lyase inhibitor
Pureté
≥97%
Propriétés du produit
ALogP
5.3
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504764185
Sourires canoniques
CCCCCCCCCC(=CC1=C(C(=O)C(=C(C1=O)OC)OC)C)C(=O)O
IUPAC Name
(2E)-2-[(4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)methylidene]undecanoic acid
InChIKey
AALSSIXXBDPENJ-FYWRMAATSA-N
INCHI
1S/C21H30O6/c1-5-6-7-8-9-10-11-12-15(21(24)25)13-16-14(2)17(22)19(26-3)20(27-4)18(16)23/h13H,5-12H2,1-4H3,(H,24,25)/b15-13+
Isomères SMILES
CCCCCCCCC/C(=C\C1=C(C(=O)C(=C(C1=O)OC)OC)C)/C(=O)O
Poids moléculaire
378.46
Reaxy-Rn
24609616
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24609616&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClassePrenol lipids
SubclassQuinone and hydroquinone lipids
Intermediate Tree Nodes Prenylquinones
Direct ParentUbiquinones
Alternative Parents P-benzoquinones  Medium-chain fatty acids  Methyl-branched fatty acids  Unsaturated fatty acids  Vinylogous esters  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homomonocyclic compounds
Substituents Ubiquinone skeleton - P-benzoquinone - Quinone - Medium-chain fatty acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acyl - Fatty acid - Unsaturated fatty acid - Vinylogous ester - Ketone - Cyclic ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Carbonyl group - Organic oxygen compound - Aliphatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6).
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeDateArticle
G23121170G23121170Certificate of AnalysisJun 14, 2023 E413754
G23121173G23121173Certificate of AnalysisJun 14, 2023 E413754
G23121174G23121174Certificate of AnalysisJun 14, 2023 E413754
G23121176G23121176Certificate of AnalysisJun 14, 2023 E413754
G23121178G23121178Certificate of AnalysisJun 14, 2023 E413754
G23121200G23121200Certificate of AnalysisJun 14, 2023 E413754
G23121211G23121211Certificate of AnalysisJun 14, 2023 E413754
G23121212G23121212Certificate of AnalysisJun 14, 2023 E413754
G23121216G23121216Certificate of AnalysisJun 14, 2023 E413754
G23121222G23121222Certificate of AnalysisJun 14, 2023 E413754
H2504045H2504045Certificate of AnalysisJun 14, 2023 E413754
Propriétés chimiques et physiques
SolubilitéSolubility (25°C) In vitro DMSO: 100 mg/mL (264.22 mM); Ethanol: 75 mg/mL (198.17 mM); Water: Insoluble;
Poids moléculaire378.500 g/mol
XLogP35.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count6
Rotatable Bond Count12
Exact Mass378.204 Da
Monoisotopic Mass378.204 Da
Topological Polar Surface Area89.900 Ų
Heavy Atom Count27
Formal Charge0
Complexity666.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Calculateurs de solution
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